Canonical Allele Identifier: CA1770800691
Gene: TNFRSF10A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23222466_23222467delinsAC , CM000670.2:g.23222466_23222467delinsAC GRCh38
NC_000008.10:g.23079979_23079980delinsAC , CM000670.1:g.23079979_23079980delinsAC GRCh37
NC_000008.9:g.23135924_23135925delinsAC NCBI36
NG_032107.1:g.7701_7702delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000221132.8:c.306+2289_306+2290delinsGT MANE Select ENSP00000221132.3:n.306+2289_306+2290delinsGT
ENST00000221132.7:c.306+2289_306+2290delinsGT ENSP00000221132.3:n.306+2289_306+2290delinsGT
ENST00000524158.5:c.-301+1966_-301+1967delinsGT ENSP00000428884.1:n.-301+1966_-301+1967delinsGT
ENST00000613472.1:c.31+2564_31+2565delinsGT ENSP00000480778.1:n.31+2564_31+2565delinsGT
NM_003844.3:c.306+2289_306+2290delinsGT NP_003835.3:n.306+2289_306+2290delinsGT
NM_003844.4:c.306+2289_306+2290delinsGT MANE Select NP_003835.3:n.306+2289_306+2290delinsGT